skip to main content


Title: Nickel telluride as a bifunctional electrocatalyst for efficient water splitting in alkaline medium
Designing efficient electrocatalysts has been one of the primary goals for water electrolysis, which is one of the most promising routes towards sustainable energy generation from renewable sources. In this article, we have tried to expand the family of transition metal chalcogenide based highly efficient OER electrocatalysts by investigating nickel telluride, Ni 3 Te 2 as a catalyst for the first time. Interestingly Ni 3 Te 2 electrodeposited on a GC electrode showed very low onset potential and overpotential at 10 mA cm −2 (180 mV), which is the lowest in the series of chalcogenides with similar stoichiometry, Ni 3 E 2 (E = S, Se, Te) as well as Ni-oxides. This observation falls in line with the hypothesis that increasing the covalency around the transition metal center enhances catalytic activity. Such a hypothesis has been previously validated in oxide-based electrocatalysts by creating anion vacancies. However, this is the first instance where this hypothesis has been convincingly validated in the chalcogenide series. The operational stability of the Ni 3 Te 2 electrocatalyst surface during the OER for an extended period of time in alkaline medium was confirmed through surface-sensitive analytical techniques such as XPS, as well as electrochemical methods which showed that the telluride surface did not undergo any corrosion, degradation, or compositional change. More importantly we have compared the catalyst activation step (Ni 2+ → Ni 3+ oxidation) in the chalcogenide series, through electrochemical cyclic voltammetry studies, and have shown that catalyst activation occurs at lower applied potential as the electronegativity of the anion decreases. From DFT calculations we have also shown that the hydroxyl attachment energy is more favorable on the Ni 3 Te 2 surface compared to the Ni-oxide, confirming the enhanced catalytic activity of the telluride. Ni 3 Te 2 also exhibited efficient HER catalytic activity in alkaline medium making it a very effective bifunctional catalyst for full water splitting with a cell voltage of 1.66 V at 10 mA cm −2 . It should be noted here that this is the first report of OER and HER activity in the family of Ni-tellurides.  more » « less
Award ID(s):
1710313
NSF-PAR ID:
10058577
Author(s) / Creator(s):
; ; ; ; ; ;
Date Published:
Journal Name:
Journal of Materials Chemistry A
Volume:
6
Issue:
17
ISSN:
2050-7488
Page Range / eLocation ID:
7608 to 7622
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Energy harvesting from solar and water has created ripples in materials energy research for the last several decades, complemented by the rise of Hydrogen as a clean fuel. Among these, water electrolysis leading to generation of oxygen and hydrogen, has been one of the most promising routes towards sustainable alternative energy generation and storage, with applications ranging from metal-​air batteries, fuel cells, to solar-​to-​fuel energy conversion systems. In fact, solar water splitting is one of the most promising method to produce Hydrogen without depleting fossil-​fuel based natural resources. However, the efficiency and practical feasibility of water electrolysis is limited by the anodic oxygen evolution reaction (OER)​, which is a kinetically sluggish, electron-​intensive uphill reaction. A slow OER process also slows the other half- cell reaction, i.e. the hydrogen evolution reaction (HER) at the cathode. Hence, designing efficient catalysts for OER process from earth-​abundant resources has been one of the primary concerns for advancing solar water splitting. In the Nath group we have focused on transition metal chalcogenides as efficient OER electrocatalysts. We have proposed the idea that these chalcogenides, specifically, selenides and tellurides will show much better OER catalytic activity due to increasing covalency around the catalytically active transition metal site, compared to the oxides caused by decreasing electronegativity of the anion, which in turn leads to variation of chem. potential around the transition metal center, [e.g. lowering the Ni 2+ -​-​> Ni 3+ oxidn. potential in Ni-​based catalysts where Ni 3+ is the actually catalytically active species]​. Based on such hypothesis, we have synthesized a plethora of transition metal selenides including those based on Ni, Ni-​Fe, Co, and Ni-​Co, which show high catalytic efficiency characterized by low onset potential and overpotential at 10 mA​/cm 2 [Ni 3 Se 2 - 200 - 290 mV; Co 7 Se 8 - 260 mV; FeNi 2 Se 4 -​NrGO - 170 mV (NrGO - N-​doped reduced graphene oxide)​; NiFe 2 Se 4 - 210 mV; CoNi 2 Se 4 - 190 mV; Ni 3 Te 2 - 180 mV]​. 
    more » « less
  2. Transition metal selenides have attracted intensive interest as cost-effective electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) because of the continuous thrust in sustainable energy conversion. In this article a Mn-based bifunctional electrocatalyst, MnSe, has been identified which shows efficient OER and ORR activity in alkaline medium. The catalytic activity could be further enhanced by using multiwalled carbon nanotubes (MWCNTs) which increases the charge transfer and electronic conductivity of the catalyst composite. This MnSe@MWCNT catalyst composite exhibits a very low overpotential of 290 mV at 10 mA cm −2 , which outperforms state-of-the-art RuO 2 as well as other oxide based electrocatalysts. Furthermore, the composite's facile OER kinetics was evidenced by its small Tafel slope of 54.76 mV dec −1 and low charge transfer resistance, indicating quick transport of the reactant species at the electrode interface. The MnSe@MWCNT also exhibited efficient electrocatalytic activity for ORR with an E onset of 0.94 V, which is among the best reported to date for chalcogenide based ORR electrocatalysts. More importantly, this MnSe-based ORR electrocatalyst exhibits high degree of methanol tolerance, showing no degradation of catalyst performance in the presence of copious quantities of methanol, thereby out-performing the state-of-the-art Pt electrocatalyst. The catalyst composite also exhibited exceptional functional and compositional stability for OER and ORR after a prolonged period of continuous operation in alkaline medium. The surface Raman analysis after OER revealed the retention of manganese selenide surface with evidence of oxo coordination, confirming the formation of an (oxy)selenide as the active surface for OER. Such efficient bifunctional OER and ORR activity makes this MnSe based catalyst attractive for overall electrolysis in regenerative as well as direct methanol fuel cells. 
    more » « less
  3. Water splitting has been widely considered to be an efficient way to generate sustainable and renewable energy resources in fuel cells, metal–air batteries and other energy conversion devices. Exploring efficient electrocatalysts to expedite the anodic oxygen evolution reaction (OER) is a crucial task that needs to be addressed in order to boost the practical application of water splitting. Intensive efforts have been devoted to develop mixed transition metal based chalcogenides as effective OER electrocatalysts. Herein, we have reported synthesis of a series of mixed metal selenides containing Co, Ni and Cu employing combinatorial electrodeposition, and systematically investigated how the transition metal doping affects the OER catalytic activity in alkaline medium. Energy dispersive spectroscopy (EDS) was performed to detect the elemental compositions and confirm the feasibility of compositional control of 66 metal selenide thin films. It was observed that the OER catalytic activity is sensitive to the concentration of Cu in the catalysts, and the catalyst activity tended to increase with increasing Cu concentration. However, increasing the Cu concentration beyond a certain limit led to decrease in catalytic efficiency, and copper selenide by itself, although catalytically active, showed higher onset potential and overpotential for OER compared to the ternary and quaternary mixed metal selenides. Interestingly, the best quaternary composition (Co 0.21 Ni 0.25 Cu 0.54 ) 3 Se 2 showed similar crystal structure as its parent compound of Cu 3 Se 2 with slight decrease in lattice spacings of (101) and (210) lattice planes (0.0222 Å and 0.0148 Å, respectively) evident from the powder X-ray diffraction pattern. (Co 0.21 Ni 0.25 Cu 0.54 ) 3 Se 2 thin film exhibited excellent OER catalytic activity and required an overpotential of 272 mV to reach a current density of 10 mA cm −2 , which is 54 mV lower than Cu 3 Se 2 , indicating a synergistic effect of transition metal doping in enhancing catalytic activity. 
    more » « less
  4. Abstract

    Designing cost‐efffective electrocatalysts for the oxygen evolution reaction (OER) holds significant importance in the progression of clean energy generation and efficient energy storage technologies, such as water splitting and rechargeable metal–air batteries. In this work, an OER electrocatalyst is developed using Ni and Fe precursors in combination with different proportions of graphene oxide. The catalyst synthesis involved a rapid reduction process, facilitated by adding sodium borohydride, which successfully formed NiFe nanoparticle nests on graphene support (NiFe NNG). The incorporation of graphene support enhances the catalytic activity, electron transferability, and electrical conductivity of the NiFe‐based catalyst. The NiFe NNG catalyst exhibits outstanding performance, characterized by a low overpotential of 292.3 mV and a Tafel slope of 48 mV dec−1, achieved at a current density of 10 mA cm2. Moreover, the catalyst exhibits remarkable stability over extended durations. The OER performance of NiFe NNG is on par with that of commercial IrO2in alkaline media. Such superb OER catalytic performance can be attributed to the synergistic effect between the NiFe nanoparticle nests and graphene, which arises from their large surface area and outstanding intrinsic catalytic activity. The excellent electrochemical properties of NiFe NNG hold great promise for further applications in energy storage and conversion devices.

     
    more » « less
  5. Abstract

    The development of efficient and robust earth‐abundant electrocatalysts for the oxygen evolution reaction (OER) is an ongoing challenge. Here, a novel and stable trimetallic NiFeCr layered double hydroxide (LDH) electrocatalyst for improving OER kinetics is rationally designed and synthesized. Electrochemical testing of a series of trimetallic NiFeCr LDH materials at similar catalyst loading and electrochemical surface area shows that the molar ratio Ni:Fe:Cr = 6:2:1 exhibits the best intrinsic OER catalytic activity compared to other NiFeCr LDH compositions. Furthermore, these nanostructures are directly grown on conductive carbon paper for a high surface area 3D electrode that can achieve a catalytic current density of 25 mA cm−2at an overpotential as low as 225 mV and a small Tafel slope of 69 mV dec−1in alkaline electrolyte. The optimized NiFeCr catalyst is stable under OER conditions and X‐ray photoelectron spectroscopy, electron paramagnetic resonance spectroscopy, and elemental analysis confirm the stability of trimetallic NiFeCr LDH after electrochemical testing. Due to the synergistic interactions among the metal centers, trimetallic NiFeCr LDH is significantly more active than NiFe LDH and among the most active OER catalysts to date. This work also presents general strategies to design more efficient metal oxide/hydroxide OER electrocatalysts.

     
    more » « less